The nitroso formed during the oxidation step was unstable and decomposed before we could isolate it.

Researchers observed that nitrosocysteine released from the endothelium caused rapid vasorelaxation in isolated arterial rings.

Nitrosoureas have been used as chemotherapy agents for certain brain tumors because they can cross the blood–brain barrier.

When the chemists oxidized aniline under mild conditions, nitrosobenzene appeared as the main product.

The nitrosonium cation (NO⁺) is often used as an electrophile in organic synthesis.

During the laboratory safety briefing, the supervisor warned that nitrosoethylurea, a highly potent mutagen with molecular formula C₃H₇N₃O₂, requires strict handling protocols.

The research team discovered that a newly synthesized nitrosourea showed potent antitumor activity in mouse models.

To investigate new reaction pathways, the chemists isolated nitrosolic acid and characterized it by NMR and mass spectrometry.

The researchers detected a nitrosothiol intermediate during the reaction and characterized its structure by NMR spectroscopy.

Researchers used nitrosoguanidine to induce mutations in bacterial cultures.